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The ICD-10-CM is a catalog of diagnosis codes used by medical professionals for medical coding and reporting in health care settings. The Centers for Medicare and Medicaid Services (CMS) maintain the catalog in the U.S. releasing yearly updates.
Clozapine is classified as an atypical antipsychotic drug because it binds to serotonin as well as dopamine receptors. Clozapine is an antagonist at the 5-HT 2A subunit of the serotonin receptor, putatively improving depression, anxiety, and the negative cognitive symptoms associated with schizophrenia.
ICD-10 code Q90. 2 for Trisomy 21, translocation is a medical classification as listed by WHO under the range - Congenital malformations, deformations and chromosomal abnormalities .
ICD-10-CM Code for Fragile X chromosome Q99. 2.
Code Z13. 89, encounter for screening for other disorder, is the ICD-10 code for depression screening.
ICD-10-CM Code for Maternal care for (suspected) chromosomal abnormality in fetus O35. 1.
ICD-10 code Z13. 40 for Encounter for screening for unspecified developmental delays is a medical classification as listed by WHO under the range - Factors influencing health status and contact with health services .
For instance, use ICD-10 code Z13. 31, “Encounter for screening for depression,” when screening for depression in patients at least 12 years old without reported symptoms. This is a preventive service defined under the Affordable Care Act and covered by many health plans.
HCPCS code G8431 for Screening for depression is documented as being positive and a follow-up plan is documented as maintained by CMS falls under Additional Quality Measures .
ICD-10 code O35. 8XX0 for Maternal care for other (suspected) fetal abnormality and damage, not applicable or unspecified is a medical classification as listed by WHO under the range - Pregnancy, childbirth and the puerperium .
Translocation Down syndrome refers to the type of Down syndrome that is caused by rearranged chromosome material. In this case, there are three # 21 chromosomes, just like there are in trisomy 21, but one of the 21 chromosomes is attached to another chromosome, instead of being separate.
Encounter for screening for global developmental delays (milestones) Z13. 42 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
Whole chromosome trisomy, mosaicism (mitotic nondisjunction) 1 Q92.1 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. 2 The 2021 edition of ICD-10-CM Q92.1 became effective on October 1, 2020. 3 This is the American ICD-10-CM version of Q92.1 - other international versions of ICD-10 Q92.1 may differ.
The 2022 edition of ICD-10-CM Q92.1 became effective on October 1, 2021.
Aneuploidy is the presence of an abnormal number of chromosomes in a cell, for example when having 45 or 47 chromosomes when 46 is expected in a human cell. It does not include a difference of one or more complete sets of chromosomes, which is called euploidy. An extra or missing chromosome is a common cause of genetic disorders, including some human birth defects. Some cancer cells also have abnormal numbers of chromosomes. Aneuploidy originates during cell division when the chromosomes do not separate properly between the two cells.
An extra or missing chromosome is a common cause of genetic disorders, including some human birth defects. Some cancer cells also have abnormal numbers of chromosomes. Aneuploidy originates during cell division when the chromosomes do not separate properly between the two cells. Specialty:
Complete trisomy 18 syndrome. Trisomy 18, complete. Clinical Information. A chromosomal abnormality consisting of the presence of a third copy of chromosome 18 in somatic cells. A kind of genetic disease.
The 2022 edition of ICD-10-CM Q91.3 became effective on October 1, 2021.
The 2022 edition of ICD-10-CM Z82.79 became effective on October 1, 2021.
Z77-Z99 Persons with potential health hazards related to family and personal history and certain conditions influencing health status